| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Center for Biological Clocks Research (M.J.B., P.D.B., R.H., D.B.P., T.L.T., V.M.C.), Department of Biology (M.J.B., P.D.B., R.H., D.B.P., T.L.T., V.M.C.), Texas A&M University, College Station, Texas 77843-3258
Address all correspondence and requests for reprints to: Vincent Cassone, Department of Biology, Texas A&M University, College Station, Texas 77843-3258. E-mail: vmc{at}mail.bio.tamu.edu.
The avian pineal gland contains both circadian oscillators and photoreceptors to produce rhythms in biosynthesis of the hormone melatonin in vivo and in vitro. The molecular mechanisms for melatonin biosynthesis are largely understood, but the mechanisms driving the rhythm itself or the photoreceptive processes that entrain the rhythm are unknown. We have produced cDNA microarrays of pineal gland transcripts under light-dark and constant darkness conditions. Rhythmic transcripts were classified according to function, representing diverse functional groups, including phototransduction pathways, transcription/translation factors, ion channel proteins, cell signaling molecules, and immune function genes. These were also organized relative to time of day mRNA abundance in light-dark and constant darkness. The transcriptional profile of the chick pineal gland reveals a more complex form of gene regulation than one might expect from a gland whose sole apparent function is the rhythmic biosynthesis of melatonin. The mRNAs encoding melatonin biosynthesis are rhythmic as are many orthologs of mammalian "clock genes." However, the oscillation of phototransductive, immune, stress response, hormone binding, and other important processes in the transcriptome of the pineal gland, raises new questions regarding the role of the pineal gland in circadian rhythm generation, organization, and avian physiology.
This article has been cited by other articles:
![]() |
L. A. Cogburn, T. E. Porter, M. J. Duclos, J. Simon, S. C. Burgess, J. J. Zhu, H. H. Cheng, J. B. Dodgson, and J. Burnside Functional Genomics of the Chicken A Model Organism Poult. Sci., October 1, 2007; 86(10): 2059 - 2094. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. W. Vitalini, R. M. de Paula, W. D. Park, and D. Bell-Pedersen The Rhythms of Life: Circadian Output Pathways in Neurospora. J Biol Rhythms, December 1, 2006; 21(6): 432 - 444. [Abstract] [PDF] |
||||
![]() |
G. J. Menger, K. Lu, T. Thomas, V. M. Cassone, and D. J. Earnest Circadian profiling of the transcriptome in immortalized rat SCN cells Physiol Genomics, May 11, 2005; 21(3): 370 - 381. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Gaildrat, M. Moller, S. Mukda, A. Humphries, D. A. Carter, V. Ganapathy, and D. C. Klein A Novel Pineal-specific Product of the Oligopeptide Transporter PepT1 Gene: CIRCADIAN EXPRESSION MEDIATED BY cAMP ACTIVATION OF AN INTRONIC PROMOTER J. Biol. Chem., April 29, 2005; 280(17): 16851 - 16860. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Bailey, P. D. Beremand, R. Hammer, E. Reidel, T. L. Thomas, and V. M. Cassone Transcriptional Profiling of Circadian Patterns of mRNA Expression in the Chick Retina J. Biol. Chem., December 10, 2004; 279(50): 52247 - 52254. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Bailey and V. M. Cassone Opsin Photoisomerases in the Chick Retina and Pineal Gland: Characterization, Localization, and Circadian Regulation Invest. Ophthalmol. Vis. Sci., March 1, 2004; 45(3): 769 - 775. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |